Package 42571-103-05

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 42571-103-05
Digits Only 4257110305
Product NDC 42571-103
Product ID 42571-103_34e9a6b6-450b-7d20-e063-6294a90ac831
Description

500 TABLET in 1 BOTTLE (42571-103-05)

Marketing

Marketing Status
Marketed Since 2013-06-13
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Glimepiride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34e9a6b6-450b-7d20-e063-6294a90ac831", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0342571100018", "0342571102012", "0342571101015", "0342571104016", "0342571105013", "0342571103019"], "unii": ["6KY687524K"], "rxcui": ["153842", "199245", "199246", "199247", "1361493", "1361495"], "spl_set_id": ["60e9397e-83b9-489e-9683-6f87e458bbaa"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42571-103-01)", "package_ndc": "42571-103-01", "marketing_start_date": "20130613"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42571-103-05)", "package_ndc": "42571-103-05", "marketing_start_date": "20130613"}], "brand_name": "Glimepiride", "product_id": "42571-103_34e9a6b6-450b-7d20-e063-6294a90ac831", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "42571-103", "generic_name": "Glimepiride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA091220", "marketing_category": "ANDA", "marketing_start_date": "20130613", "listing_expiration_date": "20261231"}